Update on the molecular genetics of vascular anomalies

Lymphatic Research and Biology

Volumn 3, Issue 4, 2005, Pages 226-233

  Wang, Qing K ^a,b  

^a LERNER RESEARCH INSTITUTE   (United States)

^b HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ENDOGLIN; GENE PRODUCT; NOTCH3 RECEPTOR; PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE; PROTEIN AGGF1; RAP1 PROTEIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR FOXC2; TRANSCRIPTION FACTOR SOX18; UNCLASSIFIED DRUG; VASCULOTROPIN RECEPTOR 3;

ANGIOGENESIS; ANGIOOSTEOHYPERTROPHY SYNDROME; ARTICLE; CADASIL; CEREBROVASCULAR MALFORMATION; CHROMOSOME TRANSLOCATION; CONGENITAL BLOOD VESSEL MALFORMATION; GENE IDENTIFICATION; GENE LOCUS; GENE MAPPING; GENETIC PREDISPOSITION; GENETIC RISK; GENETIC SUSCEPTIBILITY; HEREDITY; HUMAN; LYMPHEDEMA; MOLECULAR GENETICS; MOLECULAR MECHANICS; MULTIPLE CANCER; PATHOGENESIS; PRIORITY JOURNAL;

ARTERIOVENOUS MALFORMATIONS; HUMANS; NEOPLASMS, VASCULAR TISSUE;

EID: 30944443213     PISSN: 15396851     EISSN: None     Source Type: Journal    
DOI: 10.1089/lrb.2005.3.226     Document Type: Article

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